| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0387-7604(88)80037-8 |
| P698 | PubMed publication ID | 3285723 |
| P2093 | author name string | Willemse J | |
| Gooskens RH | |||
| Hanlo PW | |||
| Bijlsma JB | |||
| P2860 | cites work | A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly | Q28240587 |
| Attempted abortion with aminopterin (4-amino-pteroylglutamic acid); malformations of the child | Q78538578 | ||
| The syndromes of Marshall and Weaver. | Q33667960 | ||
| Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia. | Q34718558 | ||
| Normal children with large heads--benign familial megalencephaly | Q34987559 | ||
| Megalencephaly; a report of two cases | Q36006114 | ||
| 1977 Edward B. D. Neuhauser lecture: neurofibromatosis in children | Q37761634 | ||
| Cryptorchidism, chest deformities, and other congenital anomalies in three brothers | Q39495617 | ||
| Megalencephaly: types, clinical syndromes, and management | Q39706397 | ||
| Clinical definition of the Hurler-Hunter phenotypes. A review of 50 patients | Q39883272 | ||
| Macrocephaly in association with unusual cutaneous angiomatosis | Q39953281 | ||
| Mannosidosis: Pathology of the Nervous System | Q40092485 | ||
| Neuroanatomical and Electroencephalographic Correlations in Sanfilippo Syndrome, Type A | Q40187626 | ||
| Megalencephaly in infants and children. The possible role of increased dural sinus pressure | Q40220490 | ||
| Hypomelanosis of Ito. Case report with involvement of the central nervous system and review of the literature | Q40239290 | ||
| Von Recklinghausen neurofibromatosis | Q40262766 | ||
| The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections | Q40273172 | ||
| Hereditary spongiform dystrophy in young children (Canavan: van Bogaert-Bertrand) | Q41078003 | ||
| Dysplastic gangliocytoma (Lhermitte-Duclos disease) of the cerebellum. Case report | Q41351809 | ||
| Unilateral megalencephaly, cerebral cortical dysplasia, neuronal hypertrophy, and heterotopia: Cytomorphometric, fluorometric cytochemical, and biochemical analyses | Q41433670 | ||
| Unilateral megalencephaly with nerve cell hypertrophy. An anatomical and quantitative histochemical study | Q42443643 | ||
| Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases | Q45159053 | ||
| Infantile spasms associated with hemihypsarrhythmia and hemimegalencephaly | Q48142163 | ||
| Unilateral megalencephaly: hamartoma or neoplasm? | Q48461449 | ||
| Cerebrospinal fluid dynamics in megalencephaly | Q48492366 | ||
| Neurologic manifestations of the organoid nevus syndrome | Q48513276 | ||
| Hemimegalencephaly--a case for hemispherectomy? | Q48526205 | ||
| Familial megalencephaly or hydrocephalus? | Q48572545 | ||
| Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues | Q48617238 | ||
| Megalencephaly in children: Clinical syndromes, genetic patterns, and differential diagnosis from other causes of megalocephaly | Q48761312 | ||
| Hypomelanosis of Ito (incontinentia pigmenti achromians)--a clinicopathologic study: macrocephaly and gray matter heterotopias | Q48899139 | ||
| Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG family | Q48934023 | ||
| Neurological abnormalities in achondroplastic children | Q51207736 | ||
| MEGALENCEPHALY; A CLINICAL STUDY WITH CHROMOSOMAL ANALYSIS. | Q51274943 | ||
| Megalencephaly, internal hydrocephalus and other neurological aspects of achondroplasia. | Q51300327 | ||
| Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly. | Q51314573 | ||
| Megalencephaly associated with hyaline pan-neuropathy. | Q51347347 | ||
| Sotos syndrome--autosomal dominant inheritance substantiated. | Q52081914 | ||
| Endocardial fibroelastosis, neurologic dysfunction and unusual facial appearance in two brothers, coincidentally associated with dominantly inherited macrocephaly. | Q52106010 | ||
| The Weaver syndrome: a rare type of primordial overgrowth. | Q52291816 | ||
| Computed tomography in the diagnosis of Canavan's disease. | Q52293100 | ||
| Macrocephaly with head growth parallel to normal growth pattern: neurological, developmental, and computerized tomography findings in full-term infants. | Q52297602 | ||
| Campomelic dysplasia. Further elucidation of a distinct entity. | Q52299172 | ||
| Lhermitte-Duclos disease (diffuse hypertrophy of the cerebellum). Report of two cases | Q52300311 | ||
| Morquio's disease and mucopolysaccharide excretion. | Q53864077 | ||
| Cerebrospinal fluid dynamics and cerebrospinal fluid infusion in children. Part II: Clinical application of lumbar cerebrospinal fluid infusion in children with macrocephaly and normal growth rate of the head circumference. | Q54446089 | ||
| I-cell disease: a clinical picture. | Q54775428 | ||
| Alexander disease: clinical, electrodiagnostic and radiographic studies | Q70838076 | ||
| Children with large heads: a practical approach to diagnosis in 557 children, with special reference to 109 children with megalencephaly | Q70907253 | ||
| CNS dysplasia in dysencephalia splanchnocystica (Gruber's syndrome). A case report | Q71384440 | ||
| [Clinical and anatomical findings in hemi-megalencephaly; role of cerebral hyperplasia and of local gigantism associated with phacomatosis] | Q73945890 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | megalencephaly | Q10748814 |
| P304 | page(s) | 1-7 | |
| P577 | publication date | 1988-01-01 | |
| P1433 | published in | Brain and Development | Q15750896 |
| P1476 | title | Megalencephaly: definition and classification | |
| P478 | volume | 10 |
| Q33735614 | Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease |
| Q63502718 | Expression of cholecystokinin, enkephalin, galanin and neuropeptide Y is markedly changed in the brain of the megencephaly mouse |
| Q48449249 | Megalencephaly and leukodystrophy with mild clinical course: a report on 12 new cases |
| Q48844262 | Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain |
| Q48090607 | The megencephaly mouse has disturbances in the insulin-like growth factor (IGF) system |
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